Pyridyl substituted thioalkyl-and oxyalkyl-thioureas and ureas

ABSTRACT

The compounds are pyridyl substituted thioalkyl-and oxyalkylthioureas and ureas which are inhibitors of histamine activity.

United States Patent Durant et al.

PYRIDYL SUBSTITUTED THIOALKYL-AND OXYALKYL-THIOUREAS AND UREAS Inventors: Graham John Durant, Welwyn Garden City; John Colin Emmett, Codicote; Charon Robin Ganellin, Welwyn Garden City, all of England Assignee: Smith Kline & French Laboratories Limited, Welwyn Garden City, England Filed: Mar. 13, 1974 Appl. No.: 450,937

Related [1.8. Application Data Continuation-impart of Scri No 290,584, Sept. 20, 1972. abandoned. which is a continuation-impart of Scr. No. 230,451, Feb. 29, 1972 abandoned.

US. Cl. i. 260/294.8 H; 260/295 E; 260/2955 D; 260/294.8 G; 424/263; 424/266 Int. Cl. C07D 213/44 Sept. 16, 1975 [58] Field of Search... 260/294.8 H, 295 E, 295.5 D

[56] References Cited UNITED STATES PATENTS 3 736,33l 5/1973 Black et al .l 260/309 1759944 9/l973 Black et al .0 260/309 OTHER PUBLICATIONS Roberts et a1. Basic Principles of Organic Chemistry, Benjamin Publishers, page 806, (1965) QD 25] RS8 C6.

Primary Examiner-Alan L. Rotman Allurney, Agent, or Firm-Joan S. Keps; Richard D. Foggio; William H. Edgerton [57] ABSTRACT PYRIDYL SUBSTITUTED THIOALKYL-AND OXYALKYL-THIOUREAS AND UREAS This application is a continuation-in-part of Ser. No. 290.584 filed Sept. 20. 1972. now abandoned. which is a continuation-in-part of Scr. No. 230,451 filed Feb. 29. l972. now abandoned.

This invention relates to pharmacologically active compounds. to pharmaceutical compositions and to methods of inhibiting H-2 histamine receptors. The compounds of the invention can exist as the addition salts but. for convenience, reference will be made throughout this specification to the parent compounds.

lt has for long been postulated that many of the physiologically active substances within the animal body, in the course of their activity, combine with certain specific sites known as receptors. Histamine is a compound which is believed to act in such a way but. since the actions of histamine fall into more than one type. it is believed that there is more than one type of histamine receptor. The type of action of histamine which is blocked by drugs commonly called antihistamines (of which mepyramine is a typical example) is believed to involve a receptor which has been designated by Ash & Schild (Brit. J. Pharmac. 1966. 27, 427) as H-l. The

substances of the present invention are distinguished by the fact that they act at histamine H-?. receptors which. as described by Black et al. (Nature. 1972. 236. 385). are histamine receptors other than the H-1 receptor. Thus they are of utility in inhibiting certain actions of histamine which are not inhibited by the abovementioned antihistamines. The substances of this in vention may also be of utility as inhibitors of certain ac tions of gastrin.

The compounds with which the present invention is concerned may be represented by the following general formula; insofar as tautomerism affects the compounds mentioned in this specification, the numbering of the nucleus has been modified accordingly;

bly A is such that the nitrogen atom is adjacent to the carbon atom shown, Preferably X is hydrogen. methyl. bromo, amino or hydroxyl and X is hydrogen. One group of preferred compounds within the present invention is that wherein Y and E are sulphur. k is l. m is 2 and R, is methyl. Preferred compounds of this invention are N-mcthyl-N'-[2-(( 3-hydroxy2 pyridyl)methylthio)ethylIthiourea and Nmcthyl-N' [2-( lbromoQ-pyridyl )methylthio )ethyl lthiourea.

The pharmaceutical compositions of this invention comprise a pharmaceutical carrier and. as the active ingredient. a compound of Formula I, in which A is (J to 2 and the other terms are as defined therein, or a pharmaceutically acceptable acid addition salt thereof.

The methods of inhibiting H2 histamine receptors in accordance with this invention comprise administering to an animal a compound which is an active ingredient of the pharmaceutical compositions of this invention.

The compounds with which the present invention is concerned wherein Y is sulphur and k is l or 2 may be produced by processes which commence with a substance of the following general formula:

FURMlLA ll wherein A. X and X have the same significance as in Formula I except that X may not be NHR FORMULA I wherein A is such that there is formed together with the carbon atom shown a pyridine ring; X is hydrogen. lower alkyl. hydroxyl, trifluoromethyl, halogen. amino but may additionally be (CH2));01 A" is l or 2 and Q is hydroxyl. halogen or methoxy. In the first stage of these processes. the compound of Formula ll is reacted with an amino-mercaptan of the following FORMULA lll:

i Z m 2 FORMULA lll wherein m has the same significance as in Formula I. When Q is halogen. this reaction may be carried out under strongly basic conditions, for example in the presence of sodium ethoxide or sodium hydroxide. Since the substance of Formula lll is a primary amine it may be necessary to protect the amino group. for example by a phthalimido group which may subsequently be removed by acid hydrolysis or by hydrazinolysis. When is hydroxyl or halogen it is found that the reaction will take place under acidic conditions e.g. in the presence ofa halogen acid such as 48% aqueous hydrogen bromide. or a halogen acid in the presence of glacial acetic acid. When Q is mcthoxy. the reaction will also take place in the presence of 489: hydrogen bromide.

When k is zero, the corresponding first stage of the reaction is between a nucleus directly substituted with a thiol or a thione and. under acidic conditions, 3- aminopropanol or, under alkaline conditions, a 3- halopropylaminc. the amino group being protected if required in the latter case. e.g.. by a phthalimido group which may subsequently be removed by acid hydrolysis.

The product produced by these processes is of the following formula 1V. and may. of course. be in the form of the acid addition salt.

FORMULA IV wherein X. has the same significance as in formula ll and A. X k and m have the same significance as in for mula I. The free base of formula IV may be obtained from the acid addition salt by treatment with an appropriate base. eg. an alkali metal alkoxidc such as sodium ethoxidc or an inorganic base such as potassium carbonate.

The compounds of formula I. where R. is hydrogen Y is sulphur and E is sulphur may be prepared from an amine of formula IV be reaction with an acyl isothiocyanate such as benzoyl isothiocyanate in an appropriate solvent such as chloroform. Alkaline hydrolysis of these compounds. e.g.. the benzoyl derivatives where R. is C..H -,(O. with a reagent such as aqueous potassium hydroxide or aqueous potassium carbonate yields the compounds of formula I where R. is hydrogen and Y and E are sulphur.

Compounds of formula I wherein R. is hydrogen, Y is sulphur and E is sulphur may alternatively be prepared directly from the amine of formula IV by reaction at elevated temperature with the thiocyanate of ammonium or of a metal such as sodium or potassium.

The compounds of formula I where R. is lower alkyl or dialkylaminoalkyl. Y is sulphur and E is sulphur may be prepared from the amine of formula IV by reaction with an isothiocyanic ester of formula R.N=C==S in an appropriate solvent such as chloroform, ethanol, isopropanol. acetonitrile or water.

Alternatively the amine of formula IV may be convertcd by reaction with carbon disulphide to the dithiocarbamic acid of the formula:

FORMULA V wherein A. X.. X 1; and m have the same significance as in formula IV and R is hydrogen and then methylated to yield the compound of formula V wherein R is methyl. Finally. reaction of this methyl ester with an amine of formula R.MH. wherein R. is lower alkyl. yields the required compound.

In the case of compounds of formula l wherein Y is oxygen. the process for their production commences with a compound of formula VI (which may itself be formed by treatment with thionyl halide of the corre sponding alcohol resulting from the reaction of a haloalkyl heterocyclic compound and the sodium salt of a diol) FORMULA \I wherein A. X.. X and m have the same significance as in formula I. k is l or 2. k m is 3 or 4 and B is halogen. This compound may be reacted with an alkali metal azide and the resulting product reduced. e.g.. by hydrogenation over a platinum dioxide catalyst to yield an amine of formula VII in which k is l or 2.

FORMULA VII and wherein A, X X and m have the same significance as in formula I.

The amines of formula VII in which k is zero are prepared by reacting a halo-pyridine under strongly basic conditions with propylene glycol and converting the resultant 3-hydroxypropoxy compound with thionyl chloride to the corresponding 3-chloropropoxy compound which on reaction with sodium azide and reduction of the product yields the required amine.

The compounds of formula VI] may be converted to the compounds of formula I wherein Y is oxygen and E is sulphur by methods analogous to those described hereinabove for the conversion of the compounds of formula IV to those of formula I wherein both Y and E are sulphur.

Compounds of formula I wherein E is oxygen may be formed from the amines of formula lV or formula Vll by treatment thereof with an isocyanate of formula R NCO wherein R is lower alkyl, benzoyl or dialkylaminoalkyl. The compounds of formula I wherein E is oxygen and R is hydrogen may be obtained by reaction of the said amines with sodium or potassium cyanate.

As stated above, the compounds represented by formula l have been found to have pharmacological activ ity in the animal body as antagonists to certain actions of histamine which are not blocked by anthistamines such as mepyramine. For example, they have been found to inhibit selectively the histamine-stimulated secrction of gastric acid from the perfused stomachs of rats anaesthetised with urethane, at doses from 0.5 to 256 micromoles per kilogram intravenously. Similarly, the action of these compounds is demonstrated by their antagonism to the effects of histamine on other tissues which, according to the above mentioned paper of Ash & Schild, are not H-l receptors. Examples of such tissues are perfused isolated guineapig heart, isolated guinea-pig right atrium and isolated rat uterus. The compounds of the invention have also been found to inhibit the secretion of gastric acid stimulated by pentagastrin or by food. In addition to the above the compounds of the invention also show anti-inflammatory activity in conventional tests such as the rat paw oedema test at doses of about 500 micromoles/kg. subcutaneously.

The level of activity found for the compositions comprising the compounds of the present invention is illustrated by the effective dose range in the anaesthetised rat, as mentioned above of from 0.5 to 256 micromoles per kilogram, given intravenously, and also by the dose effective in the rat paw oedema test.

The pharmaceutical carrier employed may be, for example, either a solid or liquid. Exemplary of solid carriers are lactose, terra alba, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate, stearic acid and the like. Exemplary of liquid carriers are syrup, peanut oil, olive oil, water and the like.

A wide variety of pharmaceutical forms can be em ployed. Thus, if a solid carrier is used, the preparation can be tableted, placed in a hard gelatin capsule in powder or pellet form, or in the form of a troche or lozenge. The amount of solid carrier will vary widely but preferably will be from about 25 mg. to about 1 gm. If a liquid carrier is used, the preparation may be in the form of a syrup, emulsion, soft gelatin capsule, sterile injectable liquid such as an ampoule, or an aqueous or nonaqueous liquid suspension.

The pharmaceutical compositions are prepared by conventional techniques involving procedures such as mixing, granulating and compressing or dissolving the ingredients as appropriate to the desired preparation.

The active ingredient will be present in the composition in an effective amount to inhibit histamine activity. The route of administration may be orally or parenterally.

Preferably, each dosage unit will contain the active ingredient in an amount of from about 50 mg. to about 250 mg, most preferably from about mg. to about 200 mg.

The active ingredient will preferably be administered in equal doses one to three times per day. The daily dosage regimen will preferably be from about mg. to about 750 mg, most preferably from about 300 mg. to about 600 mg.

For therapeutic use, the pharmacologically active compounds of the present invention will normally be administered as a pharmaceutical composition comprising as the or an essential active ingredient at least one such compound in the basic form or in the form of an addition salt with a pharmaccutically acceptable acid and in association with a pharmaceutical carrier therefor. Such addition salts include those with hydrochloric. hydrobromic, hydriodic, sulphuric, picric and maleic acids.

Other pharmacologically active compounds may in certain cases be included in the composition. Advantageously the composition will be made up in a dosage unit form appropriate to the desired mode of administration, for example as a tablet, capsule. injectable solution or, when used as an anti-inflammatory agent, as a cream for topical administration.

The invention is illustrated but in no way limited by the following examples:

EXAMPLE I N-Methyl-N-[ 2-( Z-pyridylmethylthio )cthyl ]thiourca (i.) a. A solution of 2-hydroxymcthy1 pyridine (5.45 g.) and cysteamine hydrochloride (6.2 g.) in aqueous hydrobromic acid I ll) ml., 48% was heated under reflux overnight. After cooling, the solution was evaporated to dryness and the residual solid washed with ethanol/ether and recrystallised from aqueous ethanol to give 2-[(2-aminoethyl)thiomethyllpyridine dihydro bromide m.p. 19ll93.

b, Phthalimidoethanethiol (2 g.) was added portionwise with stirring to a solution of sodium cthoxide (prepared from 0.23 g. of sodium) in ethanol (20 ml.) at 0 under a nitrogen atmosphere. After stirring at 0 for a further 2% hours, the resulting yellow solution was cooled with an ice-salt bath and a solution of 2- chloromethylpyridine hydrochloride (0.83 g.) in ethanol (5 ml.) was added dropwise over 10 minutes. After addition the mixture was stirred at room temperature overnight. then acidified with ethanolic hydrogen chloride and evaporated to dryness. Addition of water precipitated unreacted phthalimidocthanethiol which was removed by filtration. The filtrate was concentrated 5 and basified with aqueous sodium bicarbonate solution to give 2-[(2-phthalimodoethyl)-thiomethyllpyridinc. A stirred mixture of this phthalimido derivative (0.65 g.) in aqueous hydrobromic acid (40 ml. 18%) was heated under reflux overnight. After cooling to 0, the resulting clear solution was filtered and the filtrate evaporated to dryness. Recrystallisation of the residue from aqueous ethanol gave 2-[(2-aminocthyl)-thiomethyl]pyridine dihydrobromide (0.55 g). m.p.

l9ll93.

c. A suspension of eysteamine hydrochloride l I88 g.) in ethanol (ZOU ml., dried over molecular sieves) was added portionwise at 0 to a solution of sodium ethoxide (prepared from 48 g. of sodium) in ethanol l litre) under a nitrogen atmosphere. After stirring at 0, for a further 2 hours. a solution of 2- chloromethylpyridine hydrochloride (78 g.) in ethanol (400 ml.) was added dropwise over 45 minutes while the temperature was maintained at li2. After addition. the mixture was stirred at room temperature overnight. filtered. and the filtrate acidified with concentrated hydrochloric acid. The solution was then evaporated to dryness. the residue dissolved in ethanol l li- (4 ml.) added. The reaction mixture was then heated under reflux for 1 hour and. after cooling. evaporated to dryness. The residual oil was chromatographed on a column of silica gel with ethyl acetate as eluant to give N-methyl-N'-[ 2-( Z-pyridylmethylthio )ethyl jthiourea (2.4 g.) as a clear oil.

Found: C. 49.4; H. 6.3; N. 17.3; S. 26.2; C H N S requires: C. 49.8; H. 6.3; N. 17.4;S. 26.6.)

EXAMPLES 28 By two-stage processes essentially similar to those described in Example Hi) and (ii) were produced thiourea compounds of the formula:

NHCH" cn sci-i cumu c wherein X. and the position of attachment of the side chain are as set out in the following Table 1. The solvent from which the product was crystallised and the melting point and elemental anlysis data of the product are also set out in the table together with the melting point of the corresponding intermediate TABLE 1 lnterm.

amine Product: N methyl-N-[2 *)methylthio)ethyl]thiourea salt Posn Mol- Elemental Analysis Ex. X. attach. m.p. Recryst. m.p. eeular No. of side from Formula Found required chain C H N S C H N S 2 .1- 2 |7|-3 H |.4 6.5 m 24.x 51.7 6.7 16.5 25.1 3-methyl CH. N..s. Z-p; ridyl l 6- 2 lXK-U isopropyl KZ- 5 l .R 7.1) l6.6 7 l .6 5 l .7 (1.7 16.5 25, I h-methyl CH" acetate H3 l-pyridyl 4 H 1 185-7 methanol 7s- 49.5 s: 17.3 2(15 49.8 (1.3 17.4 26.0 .l-pyridyl ether Ht) s H 4 236-8 7 49s as in 203 49x 6.; l7 4 26.6 J-pyridyl 6 3- 2 231-2 water IJU- 46.4 .9 l6. l 24.8 46.7 5.! I63 24.9 3-hydroxy- ()H I33 Z-pyridyl 7 3- 2 252-4 low .17.! 4.7 I 2 I93 37.5 4.4 [3.] 20.0 ILhrumtv Hr m.p. BrNnsl 2-p rid l solid x i- 3 210-2 water 13th t...H. 40. 5.7 m5 24.9 46.7 5+) mi 24.) s-h arm ()H 2 Nos 2-pyridyl tre) and a solution of excess picric acid in hot ethanol amine salt of formula: added. The resulting crude picrate was dissolved in water (2.7 litres) and. after decantation from an insolu ble oil. the solution was left to cool to give 2 ((2- arninoethyl )thiomethyl )pyridine dipicrate. X

Treatment of this picrate with aqueous hydrohromic (HflscHrtHflNHfl-z'la' acid followed by extraction with toluene gave the dihy N drobromide. m.p. l9ll93, after evaporation to dryness and recrystallisation of the crude residue from eth- 6U anolv ii. An aqueous solution of 2-((aminoethyl)-thiomethyl)pyridine dihydrobromide (4.95 g.) was hasified with excess solid potassium carbonate. The resultant paste was extracted with ether/ethanol (l: l) and the extracts dried and evaporated. leaving a residual amine (2.45 g.) which was dissolved in ethanol and a solution of methyl isothiocyanate l.2l g.) in isopropyl alcohol The starting materials of formula:

cn q

wherein Q is hydroxyl, halogen or methoxy are all known compounds. In each case, the starting material was reacted with cysteamine hydrochloride in aqueous hydrobromic acid as described in Example 1 (i) a. Where necessary. the resultant amine was purified by conversion to the picrate followed by treatment with hydrochloric or hydrobromic acid and removal of pieric acid, thus yielding the corresponding hydrochloride or hydrobromide, as described in Example 1 (i)(c).

Conversion of this hydrochloride or hydrobromide into the free base by the addition of potassium carbonate followed by concentration and extraction with isopropanol or ether/ethanol (3:1 yielded an extract which was reacted with methyl isothiocyanate in an appropriate solvent under conditions similar to those described in example l (ii). The resultant thiourea products, where crystallisable, were recrystallised from a solvent as indicated in table 1.

EXAMPLE 9 N-Methyl-N'-[ 3-( 2-pyridylthio )propyl lthiourea i. A solution of 2-mercaptopyridine (2.2 g.) and 3- aminopropanol (1.14 ml.) in hydrobromic acid (48%, 25 ml.) was heated under reflux for 25 hours. The reac tion mixture was evaporated to dryness and the oily re sidual solid recrystallised twice from ethanol to give 2- (3-aminopropylmercapto )pyridine dihydrobromide (3.2 g.) m.p. l86l88.

ii. This amine dihydrobromide (7 g.) was converted to the free base and reacted with methyl isothiocyanate (1.60 g.) in ethanol to give a crude yellow solid after evaporation of the reaction mixture. This crude product was chromatographed on silica gel with elution by methanol-ethyl acetate 1:3 treated with aqueous hydrochloric acid, concentrated and recrystallised from ethanol/ether to give N-methyl-N'-[3-(2-pyridylthio)- propyl]thiourea hydrochloride m.p. l40142.

Found: C, 43.4; H, 6.0; N, 15.1; S. 23.0; C1, 12.7 C H N S HCL requires: C, 43.2; H, 5.8; N, 15.1; S, 23.1; C1, 12.8).

EXAMPLE 10 N-Methyl-N-[ 2-( Z-pyridylmethylthio )ethyl ]urea A mixture of 2-[(Z-aminoethyl)thiomethyl]pyridine (7.0 g.) and methyl isocyanate (2.7 g.) in acctonitrile was heated for 18 hours in a pressure vessel at 100. After cooling, the solid obtained was collected and re crystallised from acetonitrile/ether to give N-methyl-N- '-[2-( Z-pyridylmethylthio)ethyl]urea m.p. 63-66.

EXAMPLE l l N-Methyl-N'-[2-((3-amino-2-pyridyl)methylthio)ethyljthiourea i. Lithium aluminium hydride (3.2 g.) was added in portions to a solution of ethyl3-aminopico1inate (6.8 g.) in dry ether 150 ml.) under nitrogen with stirring and cooling. After addition, the suspension was heated under reflux for 30 minutes and diluted with ether 150 ml.) then cooled during the addition of water (3.2 ml.) dilute sodium hydroxide (3.2 ml.) and water (9.6 ml.). The slurry was stirred at room temperature for 30 minutes, magnesium sulphate was added and the whole filtered, the residue being washed well with ether. Concentration followed by treatment of the residue with hydrogen chloride in ether gave 3-amino-2-hydroxymethylpyridine hydrochloride (4.2 g.) m.p. 292300.

which was recrystallised from methanolether without change in melting point.

ii. A solution of 3-amino-2-hydroxymethylpyridine hydrochloride (3.4 g.) and cysteamine hydrochloride (2.38 g.) in aqueous hydrobromic acid (50 ml. 48%) was heated under reflux for 12 hours. Concentration under reduced pressure followed by re-evaporation of the residue with ethanol gave a yellow solid g.) which was recrystallised from methanolether to afford 3-amino-2-[(2'aminoethyl)thiomethyllpyridine dihydrobromide (5.8 g.) m.p. ll96.

iii. 3-Amino-2[(Z-aminoethyl)thiomethyllpyridine (3.0 g.) prepared from an aqueous slurry of the dihydrobromide and potassium carbonate, by extraction with ethanol-ether (2:1) was dissolved in ethanol (25 ml. methyl isothiocyanate 1.16 g.) added and the solution then heated under reflux for 30 minutes. The residue was triturated with ether affording a solid (3.4 g. m.p. 98l00. Rccrystallisation from isopropyl acetate gavc N-mcthyl-N'-[2-( 3-amino-2-pyridyl )-methylthio)ethyl]thiourea in 3 crops, m.p. 99.5-l00.5 (1.33 g.), m.p. l0010l (1.04 g.) and m.p. 99l00 (1.0 g.).

Found: C, 47.2; H. 6.3; N. 21.7; S, 24.4 C,,,H ,'N,S requires: C, 46.8; H, 6.3; N. 21.9; S, 25.0)

EXAMPLE 12 In the procedure of Example 1. using in place of Z-hydroxymethylpyridine the following compounds:

Z-hydroxymethyl-5-trifluoromethylpyridine 2,4-dihydroxymethyl )pyridine Z-hydroxymethyl-4.6-dimethylpyridinc 4-chloro-2-hydroxymethyl-6-methylpyridine the products are. respectively:

N-mcthyl-N 2-( 5-trif|uoromethyl-Z-pyridyl mcthylthio )ethyl ]thiourea 2,4-bis[ 2-( N-methylthioureido )ethylthiomethyl pyridine. N-mcthyl-N-[ 2-( 4,6-dimethyl Zpyridyl methylthio )ethyl ]thiourea N-methyl-N'-[ 2-( 4-chloro-6-mcthyl-2'pyridyl methylthio )ethyl lthiourea EXAMPLE 13 N-Methyl-N'-[ 2-( 2-pyridylmethoxy )ethyl Ithiourea 2-Chloromethylpyridine is reacted with the sodium salt of ethylene glycol to give 2-(2-hydroxyethoxymethyl)-pyridine. Treatment of 2-(2-hydroxyethoxymcthyl)pyridine with thionyl chloride gives 2-(2- chloroethyoxymethyl )pyridine.

A stirred suspension of 2-( 2-chloroethoxymcthyl)- pyridine hydrochloride and sodium azide (9.8 g.) in dry dimethylformamidc (103 ml.) is maintained at 95 for 5 hours and then set aside overnight at room tempera ture. Following dilution with water and filtration, the filtrate is concentrated and the residue purified by chromatography on a dry column of alumina using ethanol. The product is basified with potassium carbonate (6.5 g.) in water (3 ml.) and the anhydrous residue is extracted with isopropyl alcohol (3 X 55 ml.). Concentration of the extracts gives 2-(2-azidoethoxymethyl)- pyridine. Hydrogenation of the azido compound in isopropyl alcohol over platinum oxide catalyst gives 2-(2- aminoethoxymethyl )pyridine.

2-( 2-Aminoethoxymethyl)pyridine is caused to react with methyl isothiocyanate 1.21 g.) in isopropyl alcohol (25 ml.) by the procedure of Example 1 to give N- methyl-N'-[Z-(Z-pyridylmethoxy)ethyll-thiourea.

EXAMPLE l4 NMethyl-N '-l 2-( 2 2-pyridyl )ethyl )thioethyl ]thi ourea Using 2-ehloroethylpyridine hydrochloride in place of Z-chloromethylpyridine hydrochloride in the procedure of Example 1 (i) (c) gives 2-((Z-aminoethyUthioethyl)pyridine dihydrobromide. Reacting this interme diate with methyl isothiocyanate by the procedure of Example 1 gives the title compound.

EXAMPLE l5 N-( Z-Dimethylaminoethyl )-N'-[ 2-( Z-pyridylmethylthio)ethyl]thiourca Treatment of 2[ Z-aminoethyl )thiomethyl ]pyridine with Z-dimethylaminoethyl isothiocyanate by the procedure of Example 1 gives the title compound.

EXAMPLE l6 N| 2-( Z-Pyridylmethylthio)ethyl lthiourea A solution of 2 [(2aminoethy|)thiomethyllpyridine (6.0 g.) and benzoyl isothiocyanate ((1.0 g.) in chloroform (I50 ml.) is heated under reflux for 1 hour and concentrated to give N benzoylN 2-( 2- pyridylmcthylthio )ethyl )thiourea.

The henzoyl thiourea is added to a solution of potassium carbonate 1.4 g.) in water (80 ml.) at 60. The solution is maintained at this temperature for 1 hour. concentrated to low bulk and acidified with hydrochlo ric acid. Bcnzoic acid is removed by filtration and the filtrate is hasified with potassium carbonate and con' centrated under reduced pressure. Following extraction with isopropyl alcohol and concentration. the product is N-l2-1Z-pyridylmcthylthio)ethyllthiourea.

EXAMPLE l7 Treatment of N-mcthylN '-l 2-(( Z-pyridyl )methylthi o)ethyl lthiourea with aqueous hydrobromic acid gives the hydrohromide salt.

The ingredients are screened. mixed and tilled into a hard gelatin capsule.

Ingredients Amounts N-Methyl-N-[ 2-( t J-hromo'Z-py ridyl methylthiolethylIthiourea Zlil) mg. Lactose ltlt) mg.

The ingredients are screened, mixed and filled into a hard gelatin capsule.

The pharmaceutical compositions prepared as in Example 18 and 19 are administered to a subject within the dose ranges given hercabove to inhibit H-2 histamine receptors.

What is claimed is: l. A compound of the formula:

wherein A is such that there is formed together with the carbon atoms shown a pyridine ring; X, is hydrogen, lower alkyl. hydroxyl, trifluoromethyl, halogen, amino X is hydrogen or. when X, is methyl, methyl or halogen, k is l or 2 and m is 2 or 3, provided that the sum ofk and m is 3 or 4; Y is oxygen or sulphur; E is oxygen or sulphur; R, is hydrogen, lower alkyl, benzoyl or di lower alkylamino-lowcr alkyl or a pharmaceutically acceptable addition salt thereof; with the proviso that X,

only when Y and E are sulphur and R, is methyl and X, is nonadjacent to the other alkylthioalkylthiourea group.

2. A compound ofclaim 1 wherein k is l and m is 2.

3. A compound of claim 1 in which X, is hydrogen, methyL bromo hydroxyl or amino and X is hydrogen; Y and E are sulphur and R, is methyl.

4. A compound of claim I. said compound being N- methy1-N'-[2-(( 3-hydroxy-2-pyridyl)methylthio)ethyl lthiourea.

5. A compound of claim 1. said compound being M- mcthyl-N '-l 2-(( 3-bromo-2-pyridyl )mcthylthio )ethyl thiourea.

6. A compound of claim 1, said compound being N- methyl-N '-l 2 t Z-pyridylmcthylthio )ethyl lthiourea.

7. A compound of claim 1, said compound being N- methyl-N'-l 2-(( 3-methyl-2-pyridyl )methylthio )ethyl]- thiourea.

8. A compound of claim 1, said compound being N- methyl-N'-[ 2-( 6-methyl-2-pyridyl )methylthio )ethyl]- thiourea.

9. A compound of claim 1, said compound being N- methyl-N 2-( 3-pyridylmethylthio )ethyl lthiourca.

It). A compound of claim 1, said compound being N- methyl-N 2-(4-pyridylmethylthio )ethyl lthiourea.

l l. A compound of claim l, said compound being N- methyl-N'-[ 2-( 2-pyridylmethylthio )ethyl ]urea.

12. A compound of claim I, said compound being N- methyl-N'[ 2-( 3-amino-2-pyridyl )methylthio )ethyl thiourea.

13. A compound of claim 1, said compound being N- methyl-N'-[ 2( S-hydroxy-Z-pyridyl )methylthio )ethyl ]thiourea.

UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATENT NO. 3,905 ,9 4 DATED September 16, 1975 INVENTOR(S) I Graham John Durant, John Colin Emmett and Charon bin Ganellin It is certifie tfiat error appears In the aboveidentified patent and that said Letters Patent are hereby corrected as shown below:

On the first page of the patent, in the left-hand column, following item [63] insert the following:

[30] Foreign Application Priority Data March 9, 1971 United Kingdom 6352/71. July 22, 1971 United Kin dom 34334/71 February 3, 1972 Ireland 13 /72 Column 10, line 6, "(3 x 55 ml.)" should read (3 x 50 ml.)

Column 11, line 60, insert EXAMPLE l9 Signed and Sealed this thirteenth D ay Of April 1 9 76 [SEAL] I A Ites t:

RUTH C. MASON (mnmissimu-r of Parents and Trademarks 

1. A COMPOUND OF THE FORMULA:
 2. A compound of claim 1 wherein k is 1 and m is
 2. 3. A compound of claim 1 in which X1 is hydrogen, methyl, bromo, hydroxyl or amino and X2 is hydrogen; Y and E are sulphur and R1 is methyl.
 4. A compound of claim 1, said compound being N-methyl-N''-(2-((3-hydroxy-2-pyridyl)methylthio)ethyl)thiourea.
 5. A compound of claim 1, said compound being M-methyl-N''-(2-((3-bromo-2-pyridyl)methylthio)ethyl)thiourea.
 6. A compound of claim 1, said compound being N-methyl-N''-(2-(2-pyridylmethylthio)ethyl)thiourea.
 7. A compound of claim 1, said compound being N-methyl-N''-(2-((3-methyl-2-pyridyl)methylthio)ethyl)thiourea.
 8. A compound of claim 1, said compound being N-methyl-N''-(2-((6-methyl-2-pyridyl)methylthio)ethyl)thiourea.
 9. A compound of claim 1, said compound being N-methyl-N''-(2-(3-pyridylmethylthio)ethyl)thiourea.
 10. A compound of claim 1, said compound being N-methyl-N''-(2-(4-pyridylmethylthio)ethyl)thiourea.
 11. A compound of claim 1, said compound being N-methyl-N''-(2-(2-pyridylmethylthio)ethyl)urea.
 12. A compound of claim 1, said compound being N-methyl-N''-(2-((3-amino-2-pyridyl)methylthio)ethyl)-thiourea.
 13. A compound of claim 1, said compound being N-methyl-N''-(2-((5-hydroxy-2-pyridyl)methylthio)ethyl)thiourea. 